FKHL20 FISH Probe
The FKHL20 FISH probe is designed to hybridize to the FKHL20 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FOXN1-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| FOXN1-20-RE | 20 (40 μL) | 200 μL |  |
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| FOXN1-20-GO | 20 (40 μL) | 200 μL |  |
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| FOXN1-20-GR | 20 (40 μL) | 200 μL |  |
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| FOXN1-20-AQ | 20 (40 μL) | 200 μL |  |
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| FOXN1-20-DIG | 20 (40 μL) | 200 μL |  |
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| FOXN1-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: FOXN1
Gene Name: Forkhead Box N1
Chromosome: CHR17: 26850958-26865175
Locus: 17q11.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FKHL20 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FOXN1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping